Abstract
Enhancer-based drug preparations allow absorption of peptid drugs.
We investigated the reversibility with time of nasal absorption of
human growth hormone (hGH) induced by the absorption enhancers
didecanoylhposphatidylcholine (DDPC) and Ó-cyclodextrin (Ó-CD).
Rabbits were dosed intranasally with enhancer in the absence of
hGH at time -3, -1, -0.5 and 0 h. At time zero the same groups of
rabbits were dosed with a hGH powder devoid of the enhancers.
Values for plasma hGH AUC and Cmax were estimated in order to
measure the degree of absorption, and rabbits receiving hGH
together with enhancers were used as positive references. With an
enhancer preparation of 8% DDPC and 30% Ó-CD, the hGH AUC and Cmax
values showed a significant time-dependent decrease after enhancer
administration. This may indicate recovery of the enhancer-induced
mucosal leakiness as well as clearance of the enhancers from the
tissue. Similar findings were obtained with Ó-CD alone, whereas a
preparation containing only DDPC showed no recovery of leakiness.
The effect of Ó-CD was also investigated in vitro in rabbit nasal
mucosa mounted in Ussing chambers. Incubation ofr 15 min with 1, 3
and 8% Ó-CD induced a concentration-dependent decrease of the
potential difference, the short circuit current and the resistance
suggesting impaired sodium transport and loosening of tight
junctions. After washout of Ó-CD, this effect was completely
reversible for the low concentrations of Ó-CD, but not for the 8%
Ó-CD. These results show that Ó-CD alone, or in combination with
DDPC, has properties as a reversible enhancer for nasal absorption
of hGH in vivo.
Original language | English |
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Journal | International Journal of Pharmaceutics |
Volume | 128 |
Pages (from-to) | 239-250 |
ISSN | 0378-5173 |
Publication status | Published - 1996 |